Product Recalls in Oregon
Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,001 recalls have been distributed to Oregon in the last 12 months.
Showing 36401–36420 of 50,914 recalls
Recalled Item: Medrad Source Administration Sets Recalled by Bayer Healthcare Due to The...
The Issue: The firm's investigation of the Medrad Intego indicates that the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter INTERLINK System Recalled by Baxter Healthcare Corp. Due to Potential...
The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corp. Due to Potential...
The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Y-Type Spike Adapter Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope (GVL) Recalled by Verathon, Inc. Due to...
The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BladderScan BVI 9600 Recalled by Verathon, Inc. Due to The firm is providing...
The Issue: The firm is providing customers with an updated Operations and Maintenance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap...
The Issue: Aesculap Inc. US has initiated a recall on Tibial and Femur extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is...
The Issue: Contamination of product with possible Bacillus spp
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bond Polymer Red Detection DS9390 kits. The common name Recalled by Leica...
The Issue: The Firm informed the importer/distributor, Leica Microsystems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Gingihue Post 5mm(D) x 5mm(P) x 2mm(H) Item: IWPP552G Dental...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Cover Screw Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Abutment and Screw Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Stop Dental implants Recalled by Biomet 3i, LLC Due to Pouches may not...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain EP Healing Abutment 5mm(D) x 5.6mm(P) x 4mm(H) Item: Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Provide Impression Coping Dental implants Recalled by Biomet 3i, LLC Due to...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Ring Abutment 4.1mm(D) x 6mm(H) Item: OSO60 Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard Abutment Pick -Up Coping Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant EP Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Pick-Up Coping 4.1mm(D) x 5mm(P) Item: IIIC12 Dental implants...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Temporary Hexed Cylinder Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.